EP2297313B1 - Alpha amylases variantes de bacillus subtilis et leurs procédés d utilisation - Google Patents

Alpha amylases variantes de bacillus subtilis et leurs procédés d utilisation Download PDF

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EP2297313B1
EP2297313B1 EP20090759577 EP09759577A EP2297313B1 EP 2297313 B1 EP2297313 B1 EP 2297313B1 EP 20090759577 EP20090759577 EP 20090759577 EP 09759577 A EP09759577 A EP 09759577A EP 2297313 B1 EP2297313 B1 EP 2297313B1
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amye
starch
seq
amylase
enzyme
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EP2297313A2 (fr
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Regina Chin
William A. Cuevas
David A. Estell
Sang-Kyu Lee
Michael J. Pepsin
Scott D. Power
Sandra W. Ramer
Carol A. Requadt
Andrew Shaw
Amr R. Toppozada
Louise Wallace
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Danisco US Inc
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Danisco US Inc
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    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/14—Hydrolases (3)
    • C12N9/24—Hydrolases (3) acting on glycosyl compounds (3.2)
    • C12N9/2402—Hydrolases (3) acting on glycosyl compounds (3.2) hydrolysing O- and S- glycosyl compounds (3.2.1)
    • C12N9/2405—Glucanases
    • C12N9/2408—Glucanases acting on alpha -1,4-glucosidic bonds
    • C12N9/2411—Amylases
    • C12N9/2414—Alpha-amylase (3.2.1.1.)
    • C12N9/2417—Alpha-amylase (3.2.1.1.) from microbiological source
    • A—HUMAN NECESSITIES
    • A21—BAKING; EDIBLE DOUGHS
    • A21D—TREATMENT, e.g. PRESERVATION, OF FLOUR OR DOUGH, e.g. BY ADDITION OF MATERIALS; BAKING; BAKERY PRODUCTS; PRESERVATION THEREOF
    • A21D8/00—Methods for preparing or baking dough
    • A21D8/02—Methods for preparing dough; Treating dough prior to baking
    • A21D8/04—Methods for preparing dough; Treating dough prior to baking treating dough with microorganisms or enzymes
    • A21D8/042—Methods for preparing dough; Treating dough prior to baking treating dough with microorganisms or enzymes with enzymes
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/38—Products with no well-defined composition, e.g. natural products
    • C11D3/386—Preparations containing enzymes, e.g. protease or amylase
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/14—Hydrolases (3)
    • C12N9/24—Hydrolases (3) acting on glycosyl compounds (3.2)
    • C12N9/2402—Hydrolases (3) acting on glycosyl compounds (3.2) hydrolysing O- and S- glycosyl compounds (3.2.1)
    • C12N9/2405—Glucanases
    • C12N9/2408—Glucanases acting on alpha -1,4-glucosidic bonds
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P19/00—Preparation of compounds containing saccharide radicals
    • C12P19/02—Monosaccharides
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P19/00—Preparation of compounds containing saccharide radicals
    • C12P19/14—Preparation of compounds containing saccharide radicals produced by the action of a carbohydrase (EC 3.2.x), e.g. by alpha-amylase, e.g. by cellulase, hemicellulase
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P7/00—Preparation of oxygen-containing organic compounds
    • C12P7/02—Preparation of oxygen-containing organic compounds containing a hydroxy group
    • C12P7/04—Preparation of oxygen-containing organic compounds containing a hydroxy group acyclic
    • C12P7/06—Ethanol, i.e. non-beverage
    • C12P7/14—Multiple stages of fermentation; Multiple types of microorganisms or re-use of microorganisms
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Y—ENZYMES
    • C12Y302/00—Hydrolases acting on glycosyl compounds, i.e. glycosylases (3.2)
    • C12Y302/01—Glycosidases, i.e. enzymes hydrolysing O- and S-glycosyl compounds (3.2.1)
    • C12Y302/01001—Alpha-amylase (3.2.1.1)
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N11/00—Investigating flow properties of materials, e.g. viscosity, plasticity; Analysing materials by determining flow properties
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E50/00—Technologies for the production of fuel of non-fossil origin
    • Y02E50/10—Biofuels, e.g. bio-diesel

Definitions

  • Alpha-amylases from Bacillus subtilis (AmyE), variants thereof, nucleic acids encoding the same, and host cells comprising the nucleic acids are described. Methods of using AmyE or variants thereof are disclosed, for ethanol production. In some cases, the amylases can be used at low pH, in the absence of calcium, and/or in the absence of a glucoamylase.
  • Grain, cereal, and vegetable starches are widely used in the industrial manufacture of products such as syrups and biofuels.
  • high fructose corn syrup HFCS
  • HFCS high fructose corn syrup
  • HFCS production currently represents a billion dollar industry.
  • the production of ethanol as a biofuel is also a growing industry.
  • Syrups and biofuels can be produced from starch by an enzymatic process that catalyzes the breakdown of starch into glucose.
  • This enzymatic process typically involves a sequence of enzyme-catalyzed reactions:
  • Maltogenic ⁇ -amylases alternatively may catalyze saccharification to form high-maltose syrups.
  • Maltogenic ⁇ -amylases typically have a higher optimal pH and a lower optimal temperature than glucoamylase, and maltogenic amylases typically require Ca 2+ .
  • Maltogenic ⁇ -amylases currently used for this application include B.subtilis ⁇ -amylases, plant amylases, and the ⁇ -amylase from Aspergillus oyzae, the active ingredient of CLARASE® L. Exemplary saccharification reactions used to produce various products are depicted below:
  • Saccharification is the rate-limiting step in the production of a glucose-rich syrup. Saccharification typically occurs over 48-72 hours, by which time many fungal glucoamylases lose significant activity. Further, although maltogenic ⁇ -amylases and glucoamylases both can catalyze saccharification, the enzymes typically operate at different optimal pH and temperatures, as shown above. If both enzymes are used sequentially, the difference in reaction conditions between the two enzymes necessitates adjusting the pH and temperature, which slows down the overall the process and may give rise to the formation of insoluble amylose aggregates.
  • compositions and methods relating to an ⁇ -amylase from Bacillus subtilis (AmyE) and related polypeptides are unique in that it exhibits high specific activity below pH 5.0, and even at about pH 4-4.5. Furthermore, Ca 2+ does not affect the thermal stability of AmyE, avoiding the need to add exogenous Ca 2+ to starch liquefaction or saccharification reactions. These features of AmyE polypeptides allow liquefaction and saccharification to be performed in the same reaction mixture (and optionally in the same reaction vessel) without the need to adjust the pH of the reaction mixture between liquefaction and saccharification.
  • reaction conditions do not have to be adjusted when using AmyE and a glucoamylase, avoiding a step and time delays between liquefaction and saccharification, along with the potential formation of insoluble amylose aggregates.
  • AmyE can, therefore, be used sequentially or simultaneously with a glucoamylase to liquefy and/or saccharify starch, and at a pH and Ca 2+ concentration that are optimal for the glucoamylase.
  • AmyE also exhibits glucoamylase activity, reducing or eliminating the need for an additional polypeptide with glucoamylase activity to perform saccharification.
  • the invention provides a method for producing ethanol from a starch substrate, comprising liquefying and saccharifying a starch substrate to produce glucose by contacting said starch substrate with an AmyE polypeptide having the sequence of SEQ ID NO: 1, SEQ ID NO: 2 or SEQ ID NO: 3, wherein the liquefaction and saccharification are performed in the same reaction mixture without a pH adjustment; said method further comprising fermenting said glucose to produce ethanol.
  • the saccharifying i.e., saccharification
  • the liquefying i.e., liquifaction
  • the pH is 5.0 or lower.
  • the pH is 4.5 or lower.
  • the pH is 4.0 or lower.
  • exogenous calcium is not added to the reaction mixture.
  • the calcium concentration in the reaction mixture is less than about 8 ppm.
  • an additional polypeptide having glucoamylase activity is added to the reaction mixture before contacting the starch substrate with the AmyE polypeptide. In some embodiments, the additional polypeptide having glucoamylase activity is added to the reaction mixture after contacting the starch substrate with the AmyE polypeptide. In some embodiments, the additional polypeptide having glucoamylase activity is added to the reaction mixture simultaneously with contacting the starch substrate with the AmyE polypeptide.
  • At least a portion of the saccharifying and fermenting occur in the same reaction mixture simultaneously, as in the case of SSF.
  • a batch fermentation process is used in a closed system, wherein the composition of the reacture mixture (including the pH) is selected at the beginning of the fermentation and is not altered during the fermentation.
  • a "fed-batch fermentation" system is used, wherein the starch substrate is added in increments as the fermentation progresses.
  • a continuous fermentation system is used, where a defined fermentation medium is added continuously to a bioreactor, and an equal amount of conditioned reaction mixture is removed for processing.
  • AmyE polypeptides are added to the reaction mixture in an amount of about 0.03-1 kg per metric ton of dry solids (ds).
  • the reaction mixture is a starch slurry having about 20-35% ds (w/w).
  • the saccharification reaction may be performed at a temperature of about 60°C to about 90°C, e.g., 70°C to 85°C, or even 10, 12, 14, 16, 18, or even 20°C below the starch gelation temperature (i.e., about 75°C), and a pH of about 4.0 to about 6.0, e.g., about 4.2 to about 4.8.
  • the product of the saccharification reaction is a glucose-rich syrup. The glucose concentration may reach at least about 95% w/w ds.
  • compositions and methods relate to an ⁇ -amylase from Bacillus subtilis (AmyE) and variants thereof (collectively referred to as AmyE polypeptides), which offer certain advantages compared to other ⁇ -amylases.
  • AmyE polypeptides exhibit high specific activity for starch substrates at an acidic pH, allowing AmyE polypeptides to be used for starch liquefaction under conditions that are also suitable for saccharification. This eliminates the need to adjust the pH of a starch slurry between liquefaction and saccharification.
  • AmyE polypeptides also posseses glucoamylase activity, eliminating or reducing the need for the use of a separate glucoamylase to perform saccharifaction.
  • starch refers to any material comprised of the complex polysaccharide carbohydrates of plants, comprised of amylose and amylopectin with the formula (C 6 H 10 O 5 ) x , wherein X can he any number.
  • the term refers to any plant-based material including but not limited to grains, grasses, tubers and roots and more specifically wheat, barley, corn, rye, rice, sorghum, brans, cassava, millet, potato, sweet potato, and tapioca.
  • oligosaccharide refers to a carbohydrate molecule composed of 3-20 monosaccharides.
  • an “amylases” refers to an enzyme capable of catalyzing the degradation of starch.
  • ⁇ -amylases EC 3.2.1.1; ⁇ -D-(1 ⁇ 4)-glucan glucanohydrolase
  • ⁇ -amylases are endoacting enzymes that cleave ⁇ -D-(1 ⁇ 4) O-glycosidic linkages within the starch molecule in a random fashion.
  • the exo-acting amylolytic enzymes such as ⁇ -amylases (EC 3.2.1.2; ⁇ -D-(1 ⁇ 4)-glucan maltohydrolase), and some product-specific amylases like maltogenic ⁇ -amylase (EC 3.2.1.133), cleave the starch molecule from the non-reducing end of the substrate.
  • amylases include any/all amylases, including glucoamylases, ⁇ -amylases, ⁇ -amylases and wild-type ⁇ -amylases, such as those of Bacillus sp., e.g., B. licheniformis and B. subtilis, while ⁇ -amylases include the aforementioned subset of these enymes.
  • ⁇ -amylase variants refer to variants/mutants of a reference ⁇ -amylase, which includes an amino acid substitution, insertion, and/or deletion with respect to the parent (wild-type; reference) amino acid sequence of the reference ⁇ -amylase.
  • variant is used interchangeably with the term "mutant.”
  • the variant ⁇ -amylase may include mutations in the signal sequence with respect to parent signal sequence.
  • the variant ⁇ -amylase can be in the form of a fusion protein containing a heterologous ⁇ -amylase signal sequence, such as from B. licheniformis (LAT).
  • LAT B. licheniformis
  • a “parent nucleic acid/polynucleotide,” “wild-type nucleic acid/polynucleotide,” or “reference nucleic acid/polynucleotide,” refers to a nucleic acid sequence encoding a parent polypeptide, and a nucleic acid complementary thereto.
  • variant nucleic acid/polynucleotide refers to a nucleic acid sequence encoding a variant polypeptide or a nucleic acid complementary thereto, or a polynucleotide sequence having at least one base substitution, insertion, or deletion with respect to a parent polynucleotide sequence or a nucleic acid complementary thereto.
  • a variant nucleic acid may be optimized to reflect preferred codon usage for a specified host organisms, such as the methylotrophic yeasts (e.g., Pichia, Hansenula, etc) or filamentous fungi ( e.g., Trichoderma ( e.g., T. reesei ), etc) or other expression hosts (e.g., Bacillus, Streptomyces, etc.).
  • a specified host organisms such as the methylotrophic yeasts (e.g., Pichia, Hansenula, etc) or filamentous fungi ( e.g., Trichoderma ( e.g., T. reesei ), etc) or other expression hosts ( e.g., Bacillus, Streptomyces, etc.).
  • a “signal sequence” is a sequence of amino acids attached to the N-terminal portion of a protein, which facilitates the secretion of the protein outside the cell.
  • the “signal sequence,” may also be referred to as a “leader sequence” or a “pro-sequence.”
  • the "immature” or “full-length (FL)" form of an amylase includes the signal peptide.
  • the immature form may include other post-translational modifications.
  • the "mature" form of an extracellular protein lacks the signal sequence.
  • the signal sequence may be cleaved off during the secretion process.
  • a polypeptide may be expressed in its mature form, e.g., as an intracellular protein, or synthesized in its mature form.
  • AmyE-tr a "truncated" form of AmyE refers to the AmyE polypeptide of SEQ NO: 2, in which the AmyE of SEQ ID NO: 1 is truncated at residue D425.
  • a 2.5 ⁇ resolution crystal structure of this AmyE-tr is available at Protein Databank Accession No. 1BAG, which is disclosed in Fujimoto et al., "Crystal structure of a catalytic-site mutant alpha-amylase from B. subtilis complexed with maltopentaose," J. Mol. Biol. 277: 393-407 (1998 ).
  • recombinant when used in reference to a subject cell, nucleic acid, protein or vector, indicates that the subject has been modified by the introduction of a heterologous nucleic acid or protein or the alteration of a native nucleic acid or protein, or that the cell is derived from a cell so modified.
  • recombinant cells express genes that are not found within the native (non-recombinant) form of the cell or express native genes that are otherwise abnormally expressed, under expressed or not expressed at all.
  • recovered refers to a compound, protein, cell, nucleic acid or amino acid that is removed from at least one component with which it is naturally associated and found in nature.
  • purified refers to material (e.g ., an isolated polypeptide or polynucleotide) that is in a relatively pure state, e.g., at least about 90% pure, at least about 95% pure, at least about 98% pure, or even at least about 99% pure.
  • thermostability refers to the ability of an enzyme to retain activity after exposure to an elevated temperature.
  • the thermostability of an enzyme is measured by its half-life (t 1/2 ) given in minutes, hours, or days, during which half the enzyme activity is lost under defined conditions.
  • the half-life may be calculated by measuring residual ⁇ -amylase activity following exposure to ( i.e., challenge by) an elevated temperature.
  • pH range refers to the range of pH values under which an enzyme exhibits catalytic activity.
  • pH stable and “pH stability” relate to the ability of an enzyme to retain activity over a wide range of pH values for a predetermined period of time (e.g., 15 min., 30 min., 1 hour, and the like).
  • amino acid sequence is synonymous with the terms “polypeptide,” “protein,” and “peptide,” and are used interchangeably. Where such amino acid sequence exhibit activity, they may be referred to as an "enzyme.”
  • amino acid sequence exhibit activity, they may be referred to as an "enzyme.”
  • the conventional one-letter or three-letter code for amino acid residues are used herein.
  • nucleic acid encompasses DNA, RNA, heteroduplexes, and synthetic molecules capable of encoding a polypeptide. Nucleic acids may be single stranded or double stranded, and may be chemical modifications. The terms “nucleic acid” and “polynucleotide” are used interchangeably. Because the genetic code is degenerate, more than one codon may be used to encode a particular amino acid, and the present compositions and methods encompass nucleotide sequences which encode a particular amino acid sequence. Unless otherwise indicated, nucleic acids are written left to right in 5' to 3' orientation; amino acid sequences are written left to right in amino to carboxy orientation, respectively.
  • homologue refers to an amino acid or nucleotide sequence having a certain degree of identity to a reference amino acid or nucleotide sequences, or another specified common structural or functional feature.
  • a homologous sequence is taken to include an amino acid sequence that is at least 75%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or even 99% identical to the subject sequence, using conventional sequence alignment tools (e.g ., Clustal, BLAST, and the like).
  • homologues will include the same active site residues as the subject amino acid sequence, unless otherwise specified.
  • hybridization refers to the process by which one strand of nucleic acid base pairs with a complementary strand, as occurs during blot hybridization techniques and PCR techniques.
  • a "degenerate sequence" in a nucleic acid contains is one in which a plurality of nucleotide sequences encode the same codon, i.e., due to the degeneracy of the genetic code. Degenerate sequences may be selected for optimal expression of an encoded polypeptide in a particular host organism, e.g., as a consequence of codon preferences.
  • a "synthetic" molecule is produced by in vitro chemical or enzymatic synthesis rather than by an organism.
  • transformed As used herein, the terms “transformed,” “stably transformed,” and “transgenic,” used with reference to a cell means that the cell has a non-native (e.g ., heterologous) nucleic acid sequence integrated into its genome or carried as an episomal plasmid that is maintained through multiple generations.
  • a non-native e.g ., heterologous
  • a “host strain” or “host cell” is an organism into which an expression vector, phage, virus, or other DNA construct including a polynucleotide encoding a polypeptide of interest (e.g., a variant ⁇ -amylase) has been introduced.
  • Exemplary host strains are bacterial cells.
  • the term "host cell” includes protoplasts created from cells, such as those of a Bacillus sp.
  • heterologous with reference to a polynucleotide or protein refers to a polynucleotide or protein that does not naturally occur in a host cell.
  • endogenous with reference to a polynucleotide or protein refers to a polynucleotide or protein that occurs naturally in the host cell.
  • expression refers to the process by which a polypeptide is produced based on the nucleic acid sequence of a gene.
  • the process includes both transcription and translation.
  • selectable marker refers to a gene capable of being expressed in a host to facilitate selection of host cells carrying the gene.
  • selectable markers include but are not limited to antimicrobials (e.g ., hygromycin, bleomycin, or neomycin) and/or genes that confer a metabolic advantage, such as a nutritional advantage on the host cell.
  • Culturing refers to growing a population of microbial cells under suitable conditions in a liquid or solid medium. Culturing includes fermentative bioconversion of a starch substrate containing granular starch to an end-product (typically in a vessel or reactor).
  • “Fermentation” is the enzymatic breakdown of organic substances by microorganisms to produce simpler organic compounds. While fermentation generally occurs under anaerobic conditions it is not intended that the term be solely limited to strict anaerobic conditions, as fermentation also occurs in the presence of oxygen.
  • a “gene” refers to a DNA segment that is involved in producing a polypeptide, and includes coding regions, regions preceding and following the coding regions, and, intervening sequences (introns) between individual coding segments (exons).
  • a “vector” refers to a polynucleotide sequence designed to introduce nucleic acids into one or more cell types.
  • Vectors include cloning vectors, expression vectors, shuttle vectors, plasmids, phage particles, cassettes and the like.
  • an "expression vector” refers to a DNA construct comprising a DNA sequence encoding a polypeptide of interest, which is operably linked to a suitable control sequence capable of effecting expression of the DNA in a suitable host.
  • control sequences may include a promoter to effect transcription, an optional operator sequence to control transcription, a sequence encoding suitable ribosome binding sites on the mRNA, enhancers and sequences which control termination of transcription and translation.
  • a “promoter” is a regulatory sequence that is involved in binding RNA polymerase to initiate transcription of a gene.
  • the promoter may be an inducible promoter or a constitutive promoter.
  • An exemplary promoter is the Bacillus licheniformis ⁇ -amylase (AmyL) promoter.
  • operably linked means that specified components are in a relationship (including but not limited to juxtaposition) permitting them to function in an intended manner.
  • a regulatory sequence is operably linked to a coding sequence such that expression of the coding sequence is under control of the regulatory sequences.
  • under transcriptional control means that transcription of a polynucleotide sequence, usually a DNA sequence, depends on its being operably linked to an element which contributes to the initiation of, or promotes transcription.
  • under translational control means that translation of a polynucleotide sequence, usually an RNA sequence, into a polypeptide depends on its being operably linked to an element which contributes to the initiation of, or promotes translation.
  • biologically active refers to a sequence having a specified biological activity, such an enzymatic activity. In the case of the present amylases, the activity is ⁇ -amylase activity.
  • Water hardness is a measure of the minerals (e.g. , calcium and magnesium) present in water.
  • “Gelatinization” refers to solubilization of a starch molecule by cooking to form a viscous suspension.
  • the term “liquefaction” or “liquefy” means a process by which starch is converted to lower molecular weight (i.e., shorter) dextrins, which are generally more soluble and less viscous than the starting starch material. This process involves gelatinization of starch simultaneously with, or followed by, the addition of AmyE or a variant thereof.
  • the term "primary liquefaction” refers to a step of liquefaction when the slurry's temperature is raised to or near its gelatinization temperature. Subsequent to the raising of the temperature, the slurry is sent through a heat exchanger or jet to temperatures from about 90-150°C, e.g., 100-110°C (200-300°F, e.g., 220-235°F. ). Subsequent to application to a heat exchange or jet temperature, the slurry is held for a period of 3-10 minutes at that temperature. This step of holding the slurry at 90-150°C (200-300°F) is termed primary liquefaction.
  • secondary liquefaction refers the liquefaction step subsequent to primary liquefaction (heating to 90-150°C (200-300°F)), when the slurry is allowed to cool to room temperature. This cooling step can be 30 minutes to 180 minutes, e.g. 90 minutes to 120 minutes.
  • minutes of secondary liquefaction refers to the time that has elapsed from the start of secondary liquefaction, to the time that the DE is measured.
  • “Saccharification” refers generally to the enzymatic conversion of maltodextrans formed after liquefaction to glucose.
  • degree of polymerization refers to the number (n) of anhydroglucopyranose units in a given saccharide.
  • DP1 are the monosaccharides, such as glucose and fructose.
  • DP2 are the disaccharides, such as maltose and sucrose.
  • a DP>3 denotes polymers with a degree of polymerization of greater than 3.
  • end-product or “desired end-product” refer to specified carbon-source-derived molecules, which are enzymatically converted from a starch substrate.
  • dry solids content refers to the total solids in a slurry, expressed in % dry weight.
  • slurry refers to an aqueous mixture containing insoluble solids.
  • residual starch refers to the remaining starch (soluble or insoluble) in a composition after fermentation or enzymatic hydrolysis of a starch containing substrate.
  • a recycling step refers to the recycling of mash components, which may include residual starch, enzymes and/or microorganisms to ferment substrates comprising starch.
  • mash refers to an aqueous mixture including a fermentable carbon source (e.g ., carbohydrate), which may be used to produce a fermented product, such as an alcohol.
  • a fermentable carbon source e.g ., carbohydrate
  • beer and “mash” may be used interchangeability.
  • stillage refers to a mixture of non-fermented solids and water, which represents the residue following removal of alcohol from a fermented mash.
  • DDG distalmost fine grain
  • DDGS distalmost fine grain with solubles
  • ethanologenic microorganism refers to a microorganism with the ability to convert a sugar or oligosaccharide to ethanol.
  • the ethanologenic microorganisms are ethanologenic by virtue of their ability to express one or more enzymes that individually or together convert sugar to ethanol.
  • ethanol producer or ethanol producing microorganism refers to any organism or cell that is capable of producing ethanol from a hexose or pentose.
  • ethanol-producing cells contain an alcohol dehydrogenase and a pyruvate decarboxylase.
  • Examples of ethanol producing microorganisms include fungal microorganisms such as yeast.
  • a preferred yeast includes strains of Sacchromyces, particularly, S. cerevisiae.
  • contacting refers to the placing of the enzyme in sufficiently close proximity to the substrate to enable the enzyme to convert the substrate to an end-product. Contacting may include mixing.
  • derived from means "originated from,” “based on,” “obtained from,” “obtainable from,” or “isolated from,” depending on context.
  • enzyme conversion generally refers to the modification of a substrate (e.g., starch) by enzyme action (e.g., amylase).
  • disintegration refers to the hydrolysis of polysaccharides in a biofilm matrix connecting and binding together individual microbial cells in the biofilm, whereby the microbial cells can be released and removed from the biofilm.
  • a “swatch” is a piece of material, such as a fabric, to which a stain may be applied for evaluating the cleaning efficiency of a composition.
  • specific activity refers to the number of moles of substrate converted to product by an enzyme preparation per unit time under specific conditions. Specific activity is expressed as units (U)/mg of protein.
  • biologically active refers to a molecule that exhibits a preselected biological function.
  • yield refers to the amount of end-product produced by a process, e.g., expressed in concentration, volume, amount, or a percentage of staring material.
  • ATCC refers to American Type Culture Collection located at Manassas, Va. 20108 (ATCC).
  • a "precipitation agent,” for purposes of purification, refers to a compound effective to precipitate a polypeptide, such as AmyE or a variant thereof, from solution.
  • the form of the precipitate may be, e.g., crystalline, amorphous, or a blend, thereof.
  • NRL refers to the Agricultural Research Service Culture Collection, National Center for Agricultural Utilization Research (and previously known as USDA Northern Regional Research Laboratory), Peoria, IL.
  • a "swatch" is a piece of material, such as a fabric, to which a stain may be applied, or which has a stain applied.
  • the material can be, for example, fabrics made of cotton, polyester or mixtures of natural and synthetic fibers.
  • the material can be paper, such as filter paper or nitrocellulose, or a piece of a hard material, such as ceramic, metal, or glass.
  • Exemplary stains include blood, milk, ink, grass, tea, wine, spinach, gravy, chocolate, egg, cheese, clay, pigment, oil, or combinations, thereof.
  • a "smaller swatch” is a piece of the swatch that has been cut with a single hole punch device, or a custom manufactured 96-hole punch device, or equivalent, where the pattern of the multi-hole punch is matched to standard 96-well microtiter plates, or has been otherwise removed from the swatch.
  • the swatch can be of textile, paper, metal, or other suitable material.
  • the smaller swatch can have the stain affixed either before or after it is placed into the well of a 24-, 48- or 96-well microtiter plate.
  • the term "food” encompasses both prepared food and ingredients for a food, such as flour, which are capable of providing a benefit to a food preparer of consumer.
  • Food ingredients includes formulations that can be added to a food or foodstuff for the purposes of, e.g., acidifying or emulsifying.
  • the food ingredient may be in the form of a solution or a solid, depending on the use and/or the mode of application and/or the mode of administration.
  • flour refers to milled or ground cereal grain or Sago or tuber products that have been ground or mashed.
  • flour may also contain components in addition to the milled or mashed cereal or plant matter, such as a leavening agent.
  • Cereal grains include wheat, oat, rye, and barley.
  • Tuber products include tapioca flour, cassava flour, and custard powder.
  • Flour also includes ground corn flour, maize-meal, rice flour, whole-meal flour, self-rising flour, tapioca flour, cassava flour, ground rice, enriched flower, and custard powder.
  • stock refers to grains and plant components that are crushed or broken.
  • barley used in beer production is a grain that has been coarsely ground or crushed to yield a consistency appropriate for producing a mash for fermentation.
  • a stock may include any of the aforementioned types of plants and grains in crushed or coarsely ground forms.
  • performance index refers to the ratio of performance of a variant polypeptide to a parent polypeptide for a specified performance characteristic.
  • up mutations refer to mutations that have a PI > 1;
  • neutral mutations refer to mutations that have a PI > 0.5;
  • non-deleterious mutations refer to mutations that have a PI > 0.05; and
  • diseleterious mutations refer to mutations that have a PI ⁇ 0.05.
  • the terms "added (or additional) glucoamylase (or glucoamylase polypeptide)" or additional polypeptide having glucoamylase activity” refers to a glucoamylase enzyme that is not the same polypeptides as AmyE.
  • AmyE polypeptide is used to refer to a polypeptide having the sequence of any one of SEQ ID NOs: 1 to 3.
  • Naturally occurring ⁇ -amylase (EC 3.2.1.1; 1,4- ⁇ -D-glucan glucanohydrolase) from B. subtilis has the sequence of SEQ ID NO: 1.
  • Amy31A polypeptide has the amino acid sequence of SEQ ID NO: 3 (Amy31A).
  • Amy31A is described in Ohdan et al., "Characteristics of two forms of alpha-amylases and structural implication," Appl. Environ. Microbiol. 65(10): 4652-58 (1999 ) and UniProtKB/TrEMBL Accession No. 082953 (SEQ ID NO: 3).
  • Amy31A has about 86% sequence identity to the AmyE of SEQ ID NO: 1, using the BLAST algorithm.
  • the AmyE amino acid sequence set forth in SEQ ID NO: 1 is that of a mature form, which lacks the native signal sequence.
  • the mature form of an AmyE is referred to elsewhere as "AmyE full-length.”
  • the native signal sequence of this AmyE is 41 amino acid residues in length and is shown as SEQ ID NO: 9.
  • the N-terminal 45 amino acid residues of SEQ ID NO: 3 are the signal sequence of Amy31A.
  • a sequence alignment between AmyE (SEQ ID NO: 1) and Amy31A (without the signal sequence) is depicted in FIG. 1 .
  • a truncated AmyE polypeptide has the amino acid sequence of SEQ ID NO: 2 (AmyE-tr). This polypeptide is truncated from residue D425 (referring to SEQ ID NO: 1).
  • a 2.5 ⁇ resolution crystal structure of AmyE-tr is available at Protein Databank Accession No. 1BAG, which is disclosed in Fujimoto et al. (1998) "Crystal structure of a catalytic-site mutant alpha-amylase from B. subtilis complexed with maltopentaose," J. Mol. Biol. 277:393-407 .
  • a DNA sequence encoding an AmyE polypeptide can be expressed, in enzyme form, using an expression vector which typically includes control sequences encoding a suitable promoter, operator, ribosome binding site, translation initiation signal, and, optionally, a repressor gene or various activator genes.
  • Vectors comprising the nucleic acids encoding AmyE or variants thereof also are provided.
  • Host cells comprising the vectors are provided.
  • the host cell may express the polynucleotide encoding the AmyE variant.
  • the host may be a Bacillus sp., e.g., B. subtilis.
  • compositions and methods include polynucleotides encoding AmyE polypeptides, as well as vectors and host cells useful for expressing AmyE polypeptides based on such polynucleotides.
  • Nucleic acids encoding AmyE polypeptides include, but are not limited to, the polynucleotides of SEQ ID NO: 5 and SEQ ID NO: 6, which encode the AmyE of SEQ ID NO: 1 and AmyE-tr (SEQ ID NO: 2), respectively, and variants thereof.
  • Further representative polynucleotides include that of SEQ ID NO: 7, which encodes Amy31A (SEQ ID NO: 3). The AmyE disclosed in NCBI Accession Nos.
  • Nucleic acids may be DNA, mRNA, or cDNA sequences. Nucleic acids further include degenerate sequences corresponding to any of the aforementioned nucleic acids. Degenerate sequences may be designed for optimal expression by using codons preferred by a particular host organism.
  • Recombinant expression vector carrying DNA sequence encoding AmyE polypeptides may be any vector that may conveniently be subjected to recombinant DNA procedures, and the choice of vector will often depend on the host cell into which it is to be introduced.
  • the vector may be an autonomously replicating vector, i.e., a vector that exists as an extrachromosomal entity, the replication of which is independent of chromosomal replication, e.g., a plasmid, a bacteriophage or an extrachromosomal element, mini-chromosome or an artificial chromosome.
  • the vector may be one which, when introduced into a host cell, is integrated into the host cell genome and replicated together with the chromosome(s) into which it has been integrated.
  • the integrated gene may also be amplified to create multiple copies of the gene in the chromosome by use of an amplifiable construct driven by antibiotic selection or other selective pressure, such as an essential regulatory gene or by complementation of an essential metabolic pathway gene.
  • An expression vector typically includes the components of a cloning vector, e.g., an element that permits autonomous replication of the vector in the selected host organism and one or more phenotypically detectable markers for selection purposes.
  • the expression vector normally comprises control nucleotide sequences encoding a promoter, operator, ribosome binding site, translation initiation signal and optionally, a repressor gene or one or more activator genes.
  • all the signal sequences used target the material to the cell culture media for easier enzyme collection and optionally purification.
  • the DNA sequence should be operably connected to a suitable promoter sequence.
  • the promoter may be any DNA sequence that shows transcriptional activity in the host cell of choice and may be derived from genes encoding proteins either homologous or heterologous to the host cell.
  • Suitable promoters for directing the transcription of the DNA sequence encoding an AmyE or variant thereof, especially in a bacterial host include various Bacillus -derived promoters, such as an ⁇ -amylase promoter derived from B.subtilis, B. licheniformis, B. stearothermophilus, or B. amyloliquefaciens, the promoter of the lac operon of E.
  • coli the Streptomyces coelicolor agarase gene dagA or celA promoters, and the promoters of the Bacillus subtilis xyl A and xylB genes, etc.
  • useful promoters are those derived from the gene encoding Aspergillus oryzae TAKA amylase, Rhizomucor miehei aspartic proteinase, Aspergillus niger neutral ⁇ -amylase, A. niger acid stable ⁇ -amylase, A. niger glucoamylase, Rhizomucor miehei lipase, A. oryzae alkaline protease, A.
  • a suitable promoter can be selected, for example, from a bacteriophage promoter including a T7 promoter and a phage lambda promoter.
  • suitable promoters for the expression in a yeast species include but are not limited to the Gal 1 and Gal 10 promoters of Saccharomyces cerevisiae and the Pichia pastoris AOX 1 or AOX2 promoters.
  • the expression vector may also comprise a suitable transcription terminator and, in eukaryotes, polyadenylation sequences operably connected to the DNA sequence encoding the ⁇ -amylase variant. Termination and polyadenylation sequences may suitably be derived from the same sources as the promoter.
  • the vector may further comprise a DNA sequence enabling the vector to replicate in the host cell in question. Examples of such sequences are the origins of replication of plasmids pUC19, pACYC177, pU13110, pE194, pAMB1, pICatH, and pIJ702.
  • the vector may also comprise a selectable marker, e.g., a gene the product of which complements a defect in the host cell, such as the dal genes from B. subtilis or B. licheniformis, or a gene which confers antibiotic resistance, e.g., ampicillin, kanamycin, chloramphenicol or tetracyclin resistance.
  • a selectable marker e.g., a gene the product of which complements a defect in the host cell, such as the dal genes from B. subtilis or B. licheniformis, or a gene which confers antibiotic resistance, e.g., ampicillin, kanamycin, chloramphenicol or tetracyclin resistance.
  • the vector may comprise Aspergillus selection markers such as amdS, argB, niaD, and xxsC, a marker giving rise to hygromycin resistance, or the selection may be accomplished by co-transformation as known in the art. See, e.g.
  • the AmyE polypeptide may comprise a signal sequence that permits secretion of the expressed enzyme into the culture medium.
  • the signal sequence may encoded by the same gene as the AmyE.
  • the AmyE set forth in (SEQ ID NO: 1 is expressed naturally with a signal sequence and additional N-terminal amino acids having the sequence MFAKRFKTSLLPLPAGFLLLFHLVLAGPAAASAETANKSNE (SEQ ID NO: 9).
  • the signal sequence alternatively may be a B. subtilis sp. signal sequence from a different AmyE or even a different protein. Further, the signal sequence may be from a different species, e.g., B.
  • the signal sequence may be chosen to provide optimal expression of the AmyE or variant thereof in a particular host cell, for example.
  • the mature AmyE may be produced as a result of proteolytic cleavage of additional sequences from the N-terminus that are not signal sequences.
  • a 31-amino acid residue signal sequence from B. licheniformis (“LAT leader sequence") may be fused in frame with an AmyE sequence.
  • a nucleic acid encoding AmyE is operably linked to a B. licheniformis signal sequence in the expression vector shown in FIG. 2 .
  • An isolated cell is advantageously used as a host cell in the recombinant production of an AmyE or variant thereof.
  • the cell may be transformed with the DNA construct encoding the AmyE or variant thereof, optionally by integrating the DNA construct (in one or more copies) in the host chromosome. This integration is generally considered to be an advantage as the DNA sequence is more likely to be stably maintained in the cell. Integration of the DNA constructs into the host chromosome may be performed according to conventional methods, e.g., by homologous or heterologous recombination. Alternatively, the cell may be transformed with an expression vector as described above in connection with the different types of host cells.
  • suitable bacterial host organisms are Gram positive bacterial species such as Bacillaceae, including B. subtilis, B. licheniformis, B. lentus, B. brevis, B. stearothermophilus, B. alkalophilus, B. amyloliquefaciens, B. coagulans , B. lautus, B. megaterium, and B. thuringiensis; Streptomyces spp., such as S. murinus ; lactic acid bacterial species including Lactococcus spp., such as L. lactis; Lactobacillus spp., including L.
  • Gram positive bacterial species such as Bacillaceae, including B. subtilis, B. licheniformis, B. lentus, B. brevis, B. stearothermophilus, B. alkalophilus, B. amyloliquefaciens, B. coagulans , B. lautus, B. megaterium, and B. thuringiens
  • Bacillus spp. A 7-7 Bacillus spp. A 7-7, for example.
  • strains of a Gram negative bacterial species belonging to Enterobacteriaceae, including E. coli, or to Pseudomonadaceae can be selected as the host organism.
  • a suitable yeast host organism can be selected from biotechnologically relevant yeasts species, such as, but not limited to, Pichia spp., Hansenula spp., Kluyveromyces spp., Yarrowinia spp., Saccharomyces spp., including S. cerevisiae, or a species belonging to Schizosaccharomyces, such as S. pombe.
  • a strain of the methylotrophic yeast species Pichia pastoris can be used as the host organism.
  • the host organism can be a Hansenula spp.
  • Suitable host organisms among filamentous fungi include species of Aspergillus, e.g., A. niger, A. oryzae, A.
  • tubigensis A. awamori, or A. nidulans.
  • a strain of Fusarium spp. e.g., Fusarium oxysporum or Rhizomucor spp., such as R. miehei, can be used as the host organism.
  • Other suitable yeasts include Thermomyces spp. and Mucor spp.
  • Fungal cells may be transformed by a process involving protoplast formation and transformation of the protoplasts followed by regeneration of the cell wall in a manner known in the art. A suitable procedure for transforming Aspergillus host cells, for example, is described in EP 238023 .
  • a method of producing an AmyE variant may comprise cultivating a host cell as described above under conditions conducive to the production of the variant and recovering the variant from the cells and/or culture medium.
  • the medium used to cultivate the cells may be any conventional medium suitable for growing the host cell in question and obtaining expression of the AmyE variant.
  • Suitable media and media components are available from commercial suppliers or may be prepared according to published recipes, e.g., as described in catalogues of the American Type Culture Collection (ATCC).
  • Exemplary culture media include, but are not limited to, those for fed-batch fermentation performed in a three thousand liter (3,000 L) stirred tank fermentor.
  • the growth medium in that case can consist of corn steep solids and soy flour as sources of organic compounds, along with inorganic salts as a source of sodium, potassium, phosphate, magnesium and sulfate, as well as trace elements.
  • a carbohydrate source such as glucose is also part of the initial medium.
  • AmyE polypeptides secreted from the host cells may conveniently be recovered from the culture medium by well-known procedures, including separating the cells from the medium by centrifugation or filtration, and precipitating proteinaceous components of the medium by means of a salt such as ammonium sulfate, followed by the use of chromatographic procedures such as ion exchange chromatography, affinity chromatography, or the like.
  • Host cells may be cultured under suitable conditions that allow expression of the AmyE polypeptides.
  • Expression of the proteins may be constitutive such that they are continually produced, or inducible, requiring a stimulus to initiate expression.
  • protein production can be initiated when required by addition of an inducer substance, e.g., dexamethasone, IPTG, or Sepharose, to the culture medium, for example.
  • an inducer substance e.g., dexamethasone, IPTG, or Sepharose
  • Polypeptides can also be produced recombinantly in an in vitro cell-free system, such as the TNTTM (Promega) rabbit reticulocyte system.
  • a host for expressing an AmyE polypeptides can be cultured under aerobic conditions in the appropriate medium for the host. Shaking or a combination of agitation and aeration can be provided, with production occurring at the appropriate temperature for that host, e.g., from about 30°C to about 75°C, depending on the needs of the host and production of the desired ⁇ -amylase variant. Culturing can occur from about 12 to about 100 hours or greater (and any hour value there between) or more particularly from 24 to 72 hours. Typically, the culture broth is at a pH of about 5.5 to about 8.0, again depending on the culture conditions needed for the host cell relative to production of the AmyE variant.
  • the amylolytic activity of the expressed enzyme may be determined using, e.g., potato starch as substrate. This method is based on the break-down of modified potato starch by the enzyme, and the reaction is followed by mixing samples of the starch/enzyme solution with an iodine solution. Initially, a blackish-blue color is formed, but during the break-down of the starch the blue color gets weaker and gradually turns into a reddish-brown, which is compared to a colored glass standard.
  • AmyE polypeptides may be expressed as a fusion protein that comprises sequences at the N- and/or C-terminus of the mature form of AmyE that facilitate expression, detection, and/or purification, e.g., a signal sequence or a His-tag.
  • a sequence includes a signal sequence, which facilitates secretion and expression of the AmyE in a host organism. Additional amino acid residues may be cleaved from the N-terminus of an AmyE, following cleavage of the signal sequence, as discussed in Yang et al., "Nucleotide sequence of the amylase gene from Bacillus subtilis," Nucleic Acids Res. 11: 237-49 (1983 ).
  • conventional methods can be used in order to prepare a purified AmyE polypeptides. After growing a host organism in culture, a growth (or "fermentation") broth is obtained, and the microbial cells and various suspended solids, including residual raw fermentation materials, are removed by conventional separation techniques to obtain an amylase solution. Filtration, centrifugation, microfiltration, rotary vacuum drum filtration, followed by ultra-filtration, extraction or chromatography, or the like are generally used.
  • the solution is concentrated using conventional techniques until the desired enzyme level is obtained. Concentration of the enzyme containing solution may be achieved by any of the techniques discussed above. In one embodiment, rotary vacuum evaporation and/or ultrafiltration is used. Alternatively, ultrafiltration can be used.
  • Precipitation can be performed using, for example, a metal halide precipitation agent.
  • Metal halide precipitation agents include: alkali metal chlorides, alkali metal bromides and blends of two or more of these metal halides.
  • the metal halide may be selected from the group consisting of sodium chloride, potassium chloride, sodium bromide, potassium bromide and blends of two or more of these metal halides.
  • Suitable metal halides include sodium chloride and potassium chloride, particularly sodium chloride, which can further he used as a preservative. The selection of conditions of the precipitation for maximum recovery, including incubation time, pH, temperature and concentration of AmyE or variant thereof, will be readily apparent to one of ordinary skill in the art after routine testing.
  • the concentration of the metal halide precipitation agent will depend, among others, on the nature of the specific AmyE or variant thereof and on its concentration in solution.
  • the organic compound precipitating agent can include: 4-hydroxybenzoic acid, alkali metal salts of 4-hydroxybenzoic acid, alkyl esters of 4-hydroxybenzoic acid, and blends of two or more of these organic compounds.
  • the addition of said organic compound precipitation agents can take place prior to, simultaneously with or subsequent to the addition of the metal halide precipitation agent, and the addition of both precipitation agents, organic compound and metal halide, may be carried out sequentially or simultaneously.
  • U.S. Patent No. 5,281,526 to Danisco A/S for example.
  • the organic compound precipitation agents are selected from the group consisting of alkali metal salts of 4-hydroxybenzoic acid, such as sodium or potassium salts, and linear or branched alkyl esters of 4-hydroxybenzoic acid, wherein the alkyl group contains from 1 to 12 carbon atoms, and blends of two or more of these organic compounds.
  • the organic compound precipitations agents can be for example linear or branched alkyl esters of 4-hydroxybenzoic acid, wherein the alkyl group contains from 1 to 10 carbon atoms, and blends of two or more of these organic compounds.
  • Suitable organic compounds include linear alkyl esters of 4-hydroxybenzoic acid, wherein the alkyl group contains from 1 to 6 carbon atoms, and blends of two or more of these organic compounds.
  • Methyl esters of 4-hydroxybenzoic acid, propyl ester of 4-hydroxybenzoic acid, butyl ester of 4-hydroxybenzoic acid, ethyl ester of 4-hydroxybenzoic acid and blends of two or more of these organic compounds can also be used.
  • Additional organic compounds also include, but are not limited to, 4-hydroxybenzoic acid methyl ester (methyl PARABEN) and 4-hydroxybenzoic acid propyl ester (propyl PARABEN), which are also amylase preservative agents. Addition of the such an organic compound precipitation agent provides the advantage of high flexibility of the precipitation conditions with respect to pH, temperature, enzyme concentration, precipitation agent concentration, and time of incubation.
  • At least 0.01 % w/v of organic compound precipitation agent is added to the concentrated enzyme variant solution and usually at least 0.02% w/v.
  • no more than 0.3% w/v of organic compound precipitation agent is added to the concentrated enzyme variant solution and usually no more than 0.2% w/v.
  • the concentrated enzyme solution containing the metal halide precipitation agent and, in one aspect, the organic compound precipitation agent, is adjusted to a pH that necessarily will depend on the enzyme variant to be purified.
  • the pH is adjusted to a level near the isoelectric point (pI) of the amylase.
  • the pH can be adjusted within a range of about 2.5 pH units below the pI to about 2.5 pH units above the pI.
  • the ply may be adjusted accordingly if the pI of the variant differs from the wild-type pI.
  • the incubation time necessary to obtain a purified enzyme precipitate depends on the nature of the specific enzyme, the concentration of enzyme, and the specific precipitation agent(s) and its (their) concentration. Generally, the time effective to precipitate the enzyme variant is between about 1 to about 30 hours; usually it does not exceed about 25 hours. In the presence of the organic compound precipitation agent, the time of incubation can still be reduced to less than about 10 hours, and in most cases even about 6 hours.
  • the temperature during incubation is between about 4°C and about 50°C
  • the method is carried out at a temperature between about 10°C and about 45°C, and particularly between about 20°C and about 40°C.
  • the optimal temperature for inducing precipitation varies according to the solution conditions and the enzyme or precipitation agent(s) used.
  • the overall recovery of purified enzyme precipitate, and the efficiency with which the process is conducted, is improved by agitating the solution comprising the enzyme, the added metal halide and the added organic compound.
  • the agitation step is done both during addition of the metal halide and the organic compound, and during the subsequent incubation period. Suitable agitation methods include mechanical stirring or shaking, vigorous aeration, or any similar technique.
  • the purified enzyme may be further purified by conventional separation techniques, such as filtration, centrifugation, microfiltration, rotary vacuum filtration, ultrafiltration, press filtration, cross membrane microfiltration, cross flow membrane microfiltration, or the like.
  • Cross membrane microfiltration can be one method used.
  • Further purification of the purified enzyme precipitate can be obtained by washing the precipitate with water.
  • the purified enzyme precipitate may he washed with water containing the metal halide precipitation agent, for example, with water containing the metal halide and the organic compound precipitation agents.
  • expressed enzyme may accumulate in the culture broth.
  • the culture broth may be centrifuged or filtered to eliminate cells, and the resulting cell-free liquid may be used for the purification of the enzyme.
  • the cell-free broth is subjected to salting out using ammonium sulfate at about 70% saturation; the 70% saturation-precipitation fraction is then dissolved in a buffer and applied to a column such as a Sephadex G-100 column, and eluted to recover the enzyme active fraction.
  • a conventional procedure such as ion exchange chromatography may he used.
  • Purified enzymes are useful for all applications in which the enzyme are generally utilized. For example, they can be used in laundry detergents and spot removers, in the food industry, in starch processing and baking, and in pharmaceutical compositions as digestive aids. They can be made into a final product that is either liquid (solution, slurry) or solid (granular, powder).
  • the enzyme product can be recovered and a flocculating agent is added to the media in order to remove cells and cell debris by filtration or centrifugation without further purification of the enzyme.
  • AmyE polypeptides produced and purified by the methods described above can be used in a variety of useful industrial applications.
  • the enzymes possess valuable properties facilitating applications related to fabric and household care (F&HC).
  • AmyE polypeptides can be used as a component in washing, dishwashing and hard-surface cleaning detergent compositions.
  • AmyE polypeptides are also useful in the production of sweeteners and ethanol from starch, and/or for textile desizing.
  • AmyE polypeptides are particularly useful in starch-conversion processes, including starch liquefaction and/or saccharification processes, as described, for example, in WO 2005/111203 and U.S. Published Application No. 2006/0014265 (Danisco A/S). These uses of AmyE polypeptides are described in more detail below.
  • the AmyE polypeptides are utilized in starch processing/conversion for producing alcohol for fuel or drinking (i.e., potable alcohol).
  • Starch conversion generally involves the hydrolysis of a slurry of ggelatinized or granular starch into a soluble starch hydrolysate.
  • Conventional starch conversion involves three consecutive enzymatic processes: a liquefaction process, a saccharification process, and a further process to produce a desired product from glucose. In the present case, the further process is fermentation.
  • the starch to be processed may be obtained from tubers, roots, stems, legumes, cereals or whole grain. More specifically, the granular starch may be obtained from corns, cobs, wheat, barley, rye, milo, sago, cassava, tapioca, sorghum, rice, peas, bean, banana, or potatoes. Specially contemplated are both waxy and non-waxy types of corn and barley.
  • the starch may be a highly refined starch quality, for instance, at least 90%, at least 95%, at least 97%, or at least 99.5% pure.
  • the starch can be a more crude starch containing material comprising milled whole grain, including non-starch fractions such as germ residues and fibers.
  • the raw material, such as whole grain, is milled to open up the structure and allow further processing.
  • dry milling dry grinding
  • dry milling the whole kernel is milled and used. Dry milled grain may include significant amounts of non-starch carbohydrate compounds, in addition to starch.
  • wet milling gives a good separation of germ and meal (starch granules and protein) and is usually used in the production of syrups.
  • the process may be conducted in an ultrafiltration system where the retentate is held under recirculation in presence of enzymes, raw starch and water, where the permeate is the soluble starch hydrolysate.
  • the process may also be conducted in a continuous membrane reactor with ultrafiltration membranes, where the retentate is held under recirculation in presence of enzymes, raw starch and water, and where the permeate is the soluble starch hydrolysate.
  • the process may further be conducted in a continuous membrane reactor with microfiltration membranes and where the retentate is held under recirculation in presence of enzymes, raw starch and water, and where the permeate is the soluble starch hydrolysate.
  • the starch slurry to be used in any of the above aspects may have about 20% to about 55% dry solids granular starch, about 25% to about 40% dry solids granular starch, or about 30% to about 35% dry solids granular starch.
  • the enzyme variant converts the soluble starch into a soluble starch hydrolysate of the granular starch in the amount of at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91 %, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99%.
  • long-chained starch molecules present in the starch slurry are degraded into shorter branched and linear molecules (maltodextrins) by an ⁇ -amylase.
  • ⁇ -amylases are available commercially, including SPEZYME® Xtra (Genencor) and LIQUOZYME® (Novozymes).
  • the liquefaction process is generally carried out at about 105-110°C for about 5 to 10 minutes followed by 1-2 hours at 95°C.
  • the pH of liquefaction is typically between about 5.0 and about 6.2, and usually above 5.5.
  • 1 mM of calcium is typically added (40 ppm free calcium ions).
  • the liquefied starch composition will largely contain dextrins, and will have a "dextrose equivalent" (DE) of about 10-15.
  • the dextrins are typically converted, in a separate saccharification step, into dextrose, by addition of a glucoamylase (e.g., AMGTM).
  • a debranching enzyme such as an isoamylase or a pullulanase (e.g., PROMOZYME®) may also be added.
  • the pH of the slurry is typically reduced to a value below about 4.5, while maintaining the temperature at 95°C or more, such that the liquefying ⁇ -amylase is denatured. The temperature then is lowered to about 60°C, and the glucoamylase and a debranching enzyme are added to affect glucose production from dextrins.
  • the saccharification process proceeds typically for about 24 to about 72 hours.
  • the dextrose syrup may be converted into high fructose syrup using an immobilized glucose isomerase (such as SWEETZYME®), for example.
  • an immobilized glucose isomerase such as SWEETZYME®
  • the soluble starch hydrolysate of the process is subjected to conversion into high fructose starch-based syrup (HFSS), such as high fructose corn syrup (HFCS).
  • HFSS high fructose starch-based syrup
  • HFCS high fructose corn syrup
  • This conversion can be achieved using a glucose isomerase, particularly a glucose isomerase immobilized on a solid support.
  • Contemplated isomerases included the commercial products SWEETZYME®, IT (Novozymes A/S); G - ZYME® IMGI, and G-ZYME® G993, KETOMAX®, G-ZYME® G993, G-ZYME® G993 liquid, and GENSWEET® IGI.
  • Ca 2+ increases the stability of conventional ⁇ -amylases, it strongly inhibits the activity of the glucose isomerase.
  • Ca 2+ is typically removed prior to isomerization, e.g., by ion exchange, such that the level of Ca 2+ is below 3-5 ppm. This process is time consuming and expensive.
  • glucose produced by saccharification is used for fermentation to produce a fermentation product, e.g., ethanol, butanol, and other compound described herein and known in the art.
  • a typical complete process for producing ethanol from starch-containing material by fermentation comprises: (i) liquefying the starch-containing material with an AmyE or variant thereof; (ii) saccharifying the liquefied mash obtained; and (iii) fermenting the material obtained in step (ii) in the presence of a fermenting organism.
  • the process further comprises recovery of the ethanol.
  • the ethanol content reaches at least about 7%, at least about 8%, at least about 9%, at least about 10% such as at least about 11%, at least about 12%, at least about 13%, at least about 14%, at least 15%, or at least 16% ethanol.
  • the saccharification and fermentation processes may be carried out as a simultaneous saccharification and fermentation (SSF) process.
  • SSF simultaneous saccharification and fermentation
  • the temperature can be between 30°C and 35°C, particularly between 31°C and 34°C.
  • the process may be conducted in an ultrafiltration system where the retentate is held under recirculation in presence of enzymes, raw starch, yeast, yeast nutrients and water and where the permeate is an ethanol containing liquid.
  • Also contemplated is the process conducted in a continuous membrane reactor with ultrafiltration membranes and where the retentate is held under recirculation in presence of enzymes, raw starch, yeast, yeast nutrients and water and where the permeate is an ethanol containing liquid.
  • Glucose produced by saccharification may also be used for production of a fermentation product such as ethanol, butanol, citric acid, monosodium glutamate, gluconic acid, sodium gluconate, calcium gluconate, potassium gluconate, glucono delta-lactone, or sodium erythorbate.
  • a fermentation product such as ethanol, butanol, citric acid, monosodium glutamate, gluconic acid, sodium gluconate, calcium gluconate, potassium gluconate, glucono delta-lactone, or sodium erythorbate.
  • AmyE polypeptides offer several advantages when used in starch hydrolysis, which distinguish them from other ⁇ -amylases and allow for the streamlining of starch hydrolysis methods.
  • dextrins may be converted into dextrose by AmyE polypeptides under the same reaction conditions that are suitable for glucoamylases. This obviates the need to optimize the reaction mixture (e.g., slurry) pH and temperature for an ⁇ -amylase, and then adjust the reactions conditions to accommodate a glucoamylase, e.g., by reducing the pH and/or temperature of the slurry.
  • the use of AmyE in starch hydrolysis permits liquefaction and saccharification to be performed under the same slurry conditions, thereby eliminating a step in starch hydrolysis.
  • Both liquefaction and saccharifiction are performed at a single pH which may be between about 4-7, e.g., about 4-5, about 4-6, about 5-6, about 5-7, and about 6-7.
  • the single pH criterion ignores any minor changes to the pH of the reaction mixture that occur during liquefaction or saccharification, but which do not involve to the addition of acid or base to intentionally change the pH of the reaction mixture.
  • both liquefaction and saccharification can be performed at a pH below that which conventional liquefaction processes are performed, for example, a pH of less than about 5.0, less than about 4.8, less than about 4.6, less than about 4.4, less than about 4.2, or even a pH of about 4.0.
  • AmyE for liquefaction also allows the inclusion of a higher percentage of thin stillage in the starch composition used for liquefaction, for example, >50%, or even >60% of the reaction mix.
  • both liquefaction and saccharification can be performed at a temperature of about 20-105°C, for example, 60-85°C, or a temperature that is about 10, 12, 14, 16, 18, or even 20°C below the starch gelation temperature (i.e., about 75°C).
  • AmyE polypeptides catalyze the breakdown of complex sugars, such as maltose, maltotriose, and maltoheptaose, into glucose. Such an enzymatic activity is conventionally associated with glucoamylases rather than ⁇ -amylases. This activity of AmyE polypeptides allows starch hydrolysis to glucose to be performed either in the absence of a separate glucoamylase, or in the presence of a reduced amount of a glucoamylase, compared to the amount required using a conventional ⁇ -amylase.
  • AmyE polypeptides in starch hydrolysis permits liquefaction and saccharification to be performed simultaneously using a single enzyme that functions as both an ⁇ -amylase and a glucoamylase, thereby eliminating or reducing the need for separate enzymes.
  • AmyE polypeptides also require little or no Ca 2+ for stability, reducing or eliminating the need to add Ca 2+ to a liquefaction reaction. In addition to avoiding the step of adding Ca 2+ , this avoids the need to subsequently remove Ca 2+ from a slurry (e.g., by ion exchange) prior to contacting the slurry with an enzyme, which is sensitive to Ca 2+ .
  • AmyE polypeptides have a high activity towards ungelatinized starch, which can be recalcitrant to the enzymatic activity of conventional ⁇ -amylases. This permits the use of jet cooked dry milled starch for liquefaction and saccharification, where wet-milled starch is generally preferred to improve conversion efficiency.
  • AmyE is suitable for use in a liquefaction/saccharification process that is tied to fermentation, including SSF.
  • AmyE polypeptides can be used alone (e.g., as the only amylolytic enzyme in starch processing) or can be combined with other ⁇ -or ⁇ -amylases, or other enzymes to provide a "cocktail" with a broad spectrum of activity.
  • the starch may be contacted with one or more enzyme selected from the group consisting of a fungal ⁇ -amylase (EC 3.2.1.1), a bacterial ⁇ -amylase, e.g., a Bacillus ⁇ -amylase or a non-Bacillus ⁇ -amylase, or a ⁇ -amylase (EC 3.2.1.2).
  • amylolytic enzyme or a debranching enzyme such as an isoamylase (EC 3.2.1.68) or a pullulanases (EC 3.2.1.41) may be combined with AmyE polypeptides.
  • Isoamylase hydrolyses ⁇ -1,6-D-glucosidic branch linkages in amylopectin and ⁇ -limit dextrins and can be distinguished from pullulanases by the inability of isoamylase to attack pullulan and by the limited action of isoamylase on ⁇ -limit dextrins.
  • ⁇ -Amylases are exo-acting maltogenic amylases, which catalyze the hydrolysis of 1,4- ⁇ -glucosidic linkages into amylose, amylopectin, and related glucose polymers, thereby releasing maltose.
  • ⁇ -amylases have been isolated from various plants and microorganisms ( Fogarty et al., PROGRESS IN INDUSTRIAL MICROBIOLOGY, Vol. 15, pp. 112-115, 1979 ). These ⁇ -amylases are characterized by having optimum temperatures in the range from 40°C to 65°C, and optimum pH in the range from about 4.5 to about 7.0.
  • Contemplated ⁇ -amylases include, but are not limited to, ⁇ -amylase from barley SPEZYME® BBA 1500, SPEZYME® DBA, OPTIMALTTM ME, OPTIMALTTM BBA (Danisco A/S); and NOVOZYMTM WBA (Novozymes A/S).
  • AmyE polypeptides have glucoamylase activity and can be used in the absence of a separate glucoamylase.
  • glucoamylases may he added in a reduced amount compared to that required for conventional stach hydrolysis methods.
  • glucoamlyses are present in an amount of no more than (i.e., less than) 0.5 glucoamylase activity unit (AGU)/g DS (i.e., glucoamylase activity units per gram of dry solids), no more than 0.4 AGU/g DS, no more than 0.3 AGU/g DS, no more than 0.2 AGU/g DS, or even no more than 0.1 AGU/g DS.
  • AGU glucoamylase activity unit
  • a glucoamylase may be added in an amount of 0.02-2.0 AGU/g DS or 0.1-1.0 AGU/g DS, although these ranges contemplate the use of more glucoamylase than is required in combination with AmyE.
  • AmyE polypeptides are active at the same pH and temperature as glucoamylase, AmyE polypeptides may be added before or after addition of a glucoamylase, or simultaneously with a glucoamylase, e.g., by means of a cocktail including both AmyE and a glucoamylase.
  • the order and manner of addition of an ⁇ -amylase and a glucoamylase are no longer critical, permitting increased flexibility in starch hydrolysis processes.
  • Glucoamylases may be derived from a microorganism or a plant. There are various known glucoamylases of fungal and bacterial origin. Exemplary bacterial glucoamylases are Aspergillus glucoamylases, in particular A . niger G1 or G2 glucoamylase ( Boel et al. (1984), EMBO J. 3:1097-1102 ), or variants thereof, such as disclosed in WO 92/00381 and WO 00/04136 ; A. awamori glucoamylase ( WO 84/02921 ); A . oryzae glucoamylase ( Agric. Biol. Chem.
  • Aspergillus glucoamylase variants include those that enhance thermal stability: G137A and G139A ( Chen et al. (1996) Prot. Eng. 9:499-505 ); D257E and D293E/Q ( Chen et al. (1995) Prot. Eng. 8:575-582 ); N182 ( Chen et al. (1994) Biochem. J. 301:275-281 ); disulphide bonds, A246C ( Fierobe et al. (1996) Biochemistry, 35:8698-8704 ); and introduction of Pro residues in positions A435 and S436 ( Li et al. (1997) Protein Eng.
  • glucoamylases include Trichoderma reesie glucoamylase (e.g., SEQ ID NO: 3 of WO 2006/060062 ; TrGA), Talaromyces glucoamylases, in particular derived from T. emersonii ( WO 99/28448 ), T. leycettanus ( U.S. Patent No. RE 32,153 ), T. duponti, or T. thermophilus ( U.S. Patent No. 4,587,215 ).
  • Bacterial glucoamylases include glucoamylases from the genus Clostridium , in particular C.
  • thermoamylolyticum EP 135138
  • C . thermohydrosulfuricum WO 86/01831
  • Other suitable glucoamylases include those derived from Aspergillus oryzae , such as a glucoamylase having 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, or even 90% homology to the amino acid sequence shown in SEQ ID NO: 2 in WO 00/04136 .
  • glucoamylases such as AMG 200L; AMG 300 L; SANTM SUPER and AMGTM E (Novozymes); OPTIDEX® 300 (Genencor Division, Danisco US Inc.); AMIGASETM and AMIGASETM PLUS (from DSM); G-ZYME® G900 (Enzyme Bio-Systems); and G-ZYME® G990 ZR ( A . niger glucoamylase and low protease content).
  • Phytases are enzymes capable of breaking down phytic acid (phytate) found in grains and oil seeds. Phytate, as well as intermediates in its degradation, are believed to destabilize or otherwise adversely affect ⁇ -amylases, thereby reducing their efficiency. Phytases that can be used in combination with variant ⁇ -amylases are capable of hydrolyzing phytic acid under the defined conditions of the incubation and liquefaction steps. In some embodiments, the phytase is capable of liberating at least one inorganic phosphate from an inositol hexaphosphate (phytic acid).
  • phytic acid inositol hexaphosphate
  • Phytases can be grouped according to their preference for a specific position of the phosphate ester group on the phytate molecule at which hydrolysis is initiated, (e.g., as 3-phytases (EC 3.1.3.8) or as 6-phytases (EC 3.1.3.26)).
  • 3-phytases EC 3.1.3.8
  • 6-phytases EC 3.1.3.26
  • a typical example of phytase is myoinositol-hexakiphosphate-3-phosphohydrolase.
  • Phytases can be obtained from microorganisms such as fungal and bacterial organisms. Some of these microorganisms include e.g. Aspergillus (e.g., A. niger, A. terreus , A. ficum and A. fumigatus), Myceliophthora (M. thermophila), Talaromyces (T. thermophilus) Trichoderma spp (T. reesei). and Thermomyces ( WO 99/49740 ). Also phytases are available from Penicillium species, e.g., P. hordei (ATCC No. 22053), P. piceum (ATCC No. 10519), or P.
  • Penicillium species e.g., P. hordei (ATCC No. 22053), P. piceum (ATCC No. 10519), or P.
  • phytases are available from Bacillus (e.g., B. subtilis, Pseudomonas, Peniophora, E. coli, Citrobacter, Enterbacter and Buttiauxella (see WO2006/043178 ).
  • phytases are available such as NATUPHOS® (BASF), RONOZYME® P (Novozymes A/S), PHZYME® (Danisco A/S, Diversa) and FINASE® (AB Enzymes).
  • BASF BASF
  • RONOZYME® P Novozymes A/S
  • PHZYME® Danisco A/S, Diversa
  • FINASE® AB Enzymes
  • Exemplary phytases are derived from species of the bacterium Buttiauxiella.
  • Buttiauxiella spp. includes B. agrestis , B. brennerea, B. ferragutiase, B. gaviniae, B. izardii , B. noackiae , and B. warmboldiae.
  • Strains of Buttiauxella species are available from DSMZ, the German National Resource Center for Biological Material (Inhoffenstrabe 7B, 38124 Braunschweig, DE).
  • Buttiauxella sp. strain P1-29 deposited under accession number NCIMB 41248 is an example of a particularly useful strain from which a phytase may be obtained.
  • the phytase may be BP-wild type, a variant thereof (such as BP-11) described in WO 06/043178 , or a variant as described in U.S. Patent Pub. No. US20080220498, filed March 6, 2007 (see, e.g., Table 1 and SEQ ID NO: 3).
  • the phytase may also be the BP-17 variant of Buttiauxiella phytase, having the amino acid sequence of SEQ ID NO: 17, shown below, or a phytase having at least 75%, at least 80%, at least 85%, at least 88%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98% and even at least 99% sequence identity to the amino acid sequence set forth in SEQ ID NO: 17.
  • the amount (dosage) of phytase used in the incubation and/or liquefaction processes may be in the range of about 0.001 to 50 FTU/g ds, (e.g., in the range of about 0.01 to 25 FTU/g ds, about 0.01 to 15 FTU/g ds, about 0.01 to 10 FTU/g ds, about 0.05 to 15 FTU/g ds, and about 0.05 to 5.0 FTU/g.
  • AmyE polypeptides include lipases, cutinases, proteases, cellulases/hemicellulases, peroxidase, pectinase, pectine lyases, laccases, or combinations, thereof. In some cases a carbohydrate-binding domain of the type disclosed in WO 98/22613 may be used.
  • wt% weight percent
  • °C degrees Centigrade
  • H 2 O water
  • dH 2 O deionized water
  • dIH 2 O deionized water
  • Milli-Q filtration g or gm (grams); ⁇ g (micrograms); mg (milligrams); kg (kilograms); ⁇ L and ⁇ l (microliters); mL and ml (milliliters); mm (millimeters); ⁇ m (micrometer); M (molar); mM (millimolar); ⁇ M (micromolar); U (units); MW (molecular weight); sec (seconds); min(s) (minute/minutes); hr(s) (hour/hours); DO (dissolved oxygen); W/V (weight to volume); W/W (weight to weight); V/V (volume to volume); IKA (IKA Works Inc.
  • FIG. 2 depicts the vector comprising a nucleic acid encoding AmyE-tr.
  • the pHPLT vector contained the B. licheniformis LAT promoter ("Plat"), a sequence encoding the LAT signal peptide ("preLAT”'), followed by Pst I and Hpa I restriction sites for cloning.
  • "ori-pUB” is the origin of replication from pUB110;
  • reppUB is the replicase gene from pUB110,
  • neo is the neomycin/kanamycin resistance gene from pUB110;
  • bleo is the bleomycin resistance marker,
  • Tlat is the transcriptional terminator from B. licheniformis amylase.
  • Plasmid constructs for the expression of AmyE and AmyE-tr were assembled using the AmyE-encoding sequence described by Yang et al, "Nucleotide sequence of the amylase gene from Bacillus subtilis," Nucl. Acids Res. 11(2): 237-49 (1983 ).
  • Plasmid pME629.5 contains the nucleic acid encoding the full-length AmyE of SEQ ID NO: 1. The gene has a three base deletion in the sequence encoding the starch binding domain, compared to the sequence described by Yang et al.
  • AmyE-tr is truncated at position D425 of SEQ ID NO: 1.
  • AmyE-tr was designed based on a crystal structure of an AmyE variant that lacked the starch binding domain, as described in Fujimoto et al., "Crystal structure of a catalytic-site mutant alpha-amylase from Bacillus subtilis complexed with maltopentaose," J. Mol. Biol. 277: 393-407(1998 ). See also, the RCSB Protein Data Bank ⁇ Accession No. 1BAG, "Alpha-Amylase From Bacillus Subtilis Complexed With Maltopentaose.”
  • the nucleic acid encoding the AmyE polypeptide was PCR-amplified using HERCULASE® (Stratagene, La Jolla, CA, USA) and purified using a column provided in a Qiagen QIAQUIKTM PCR purification kit (Qiagen, Valencia, CA, USA), and resuspended in 50 ⁇ L of MILLI-QTM-purified water. 50 ⁇ L of the purified DNA was digested sequentially with Hpa I (Roche) and Pst I (Roche), and the resultant DNA fragments was resuspended in 30 ⁇ L of MILLI-QTM-purified water.
  • B. subtilis cells (genotype: ⁇ aprE, ⁇ nprE, degUHy32 oppA, ⁇ spoIIE3501 , amyE::xylRPxylAcomK-phleo ).
  • B. subtilis cells had a competency gene ( comK ) placed under the control of a xylose-inducible promoter. Competency for DNA binding and uptake is induced by the addition of xylose.
  • the plasmids pME629.5 and pME630.7 express AmyE with a 31 residue signal sequence, which is cleaved post-translationally. The subsequent 10 N-terminal amino acids are processed separately as proposed by Yang et al. (1983).
  • pME629.5 encodes "full-length” AmyE and pME630.7 encodes "truncated” AmyE.
  • Bacterial transformants harboring constructs encoding AmyE full-length and truncated polypeptides were selected on Luria agar (LA) with 10 ⁇ g/mL neomycin, 1% insoluble starch and incubated overnight at 37°C. Transformants showing a clearing (or halo) around the colony were selected for further studies. Precultures of each of the transformants were grown for 8 h in LB with 10 ⁇ g/mL neomycin. 30 ⁇ L of each pre-culture was added into a 250 mL flask filled with 30 mL of cultivation media (described below) supplemented with 10 ⁇ g/mL neomycin and 5 mM CaCl 2 .
  • the cultivation media was an enriched semi-defined media based on MOPs buffer, with urea as the major nitrogen source, glucose as the main carbon source, and supplemented with 1% soytone for robust cell growth.
  • the shake flasks were incubated for 60-65 hours at 37°C, with mixing at 250 rpm. Cultures were harvested by centrifugation at 5,000 rpm for 20 minutes in conical tubes. Since both AmyE full-length and AmyE truncated proteins expressed at high levels, the culture supernatants were used for subsequent assays without further purification.
  • Amylase activity was measured spectrophotometrically.
  • Insoluble corn starch covalently linked with the label Remazol Brilliant Blue R (“RBB-corn starch,” Sigma S7776) was used as a substrate.
  • a viscometer was used to measure the viscosity of a corn starch substrate in the presence of an amylase at pH 4.5 and 5.8.
  • a batch of 30% ds corn starch substrate slurry was freshly made, using sulfuric acid to lower the pH to either 4.5 or 5.8.
  • 50 g of slurry (15 g ds) was weighed out and warmed for 10 minutes to 70°C.
  • the temperature was immediately increased from 70°C to 85°C, and the reaction was stirred at 75 rpm. Once the temperature of the slurry and enzyme mixture reached 85"C, the viscosity was monitored for an additional 30 minutes.
  • the excess heat capacity function of AmyE or a variant thereof was measured in the presence or absence of 2 mM calcium chloride using an ultrasensitive scanning high-throughput microcalorimeter (VP-Capillary DSC; MicroCal, Inc., Northampton, MA, USA). Approximately 500 ⁇ L of 0.5 mg/mL of AmyE or a variant thereof were scanned over 30-120°C temperature range. Truncated Geobacillus stearothermophilus ⁇ -amylase (AmyS) was used as a control. The amino acid sequence of AmyS, including a 34 amino acid signal sequence, is shown in SEQ ID NO: 4. The same sample was then re-scanned to check the reversibility of the process.
  • the buffer used was 10 mM sodium acetate, pH 5.5.
  • a 200°C/hr scan rate was used to minimize any artifacts resulting from aggregation.
  • the thermal midpoint (T m ) of the DSC curves was used as an indicator of thermal stability. The standard error in all the T m measurements was less than 1%.
  • Protein concentration in sample supernatants was determined using the Bradford QUICKSTARTTM Dye Reagent (Bio-Rad, Hercules, CA, USA). Samples were obtained by filtering broths from cultures grown in microtiter plates (MTPs) for 3 days at 37°C with shaking at 280 rpm and humidified aeration. 10 ⁇ L of the culture filtrate was combined with 200 ⁇ L Bradford QUICKSTARTTM Dye Reagent in a well of a second MTP. After thorough mixing, the MTP were incubated for at least 10 minutes at room temperature. Air bubbles were removed and the OD (optical density) was measured at 595 nm. To determine the protein concentration, the background reading (from uninoculated wells) was subtracted from the sample readings.
  • MTPs microtiter plates
  • maltose or maltoheptaose solutions were prepared in 50 mM sodium acetate, pH 4.5 or 5.6, or in 50 mM malic acid pH 5.6, as specified for each experiment. All enzyme samples were initially diluted to 1 mg/mL. Reaction mixtures were prepared by diluting the enzyme using the appropriate substrate solutions to give a final enzyme concentration of 1 ppm, and then 200 ⁇ L aliquots were transferred to sterile screw top tubes and place in a 37°C incubator. The reactions were stopped at the indicated times by diluting 10-fold into 10 mM sodium hydroxide.
  • purified Amy E or variants thereof (24.5g/L) was diluted to a final concentration of 20.4 ppm in malic acid buffer, pH 5.6.
  • the protein was then added to a 5% corn flour solution prepared in malic acid buffer, pH 5.6, to a final concentration of 1 ppm, and the mixture was incubated in a shaker at 32°C. Samples were periodically removed and diluted 10 fold into 50 mM NaOH to quench the reaction.
  • maltose or maltoheptaose to glucose was assayed by HPLC.
  • 0.5% maltose and maltoheptaose solution were made in a 50 mM sodium acetate buffer at pH 4.5 and pH 5.6. All enzyme samples were diluted to 1 mg/mL from purified stocks. The 1 mg/mL enzyme sample was further diluted into the maltose solution to give a final concentration of 1 ⁇ g/mL enzyme. 200 ⁇ L aliquots were then added to sterile screw-top tubes and placed in a 37°C incubator. The reactions were stopped after 2, 5, and 8 days by the addition of sodium hydroxide. The formation of glucose and the breakdown of maltose were analyzed by HPLC against authentic standards, using the methods described in Example 2.5.
  • Standard total reducing sugars, glucose, and iodine assays were performed separately to characterize the products of amylopectin digestion.
  • a 2.2% (w/w) corn amylopectin substrate was prepared in 55 mM sodium acetate buffer pH 5.8 by boiling the mixture with stirring for 30 minutes and then cooling to room temperature.
  • One hundred ⁇ l of substrate was placed in wells of a 96 well medium binding polystyrene microtiter plate and 10 ⁇ l of diluted culture supernatants of AmyE variants were added to it. Plates were sealed (Nunc, cat. # 236366) and immediately placed in an iEMS shaking incubator and incubated at 50C for 10 min, 1150 rpm.
  • Amylase reactions were terminated via addition of 20 ⁇ l 0.5 N NaOH with mixing.
  • Total reducing sugars present were determined by mixing 20 ⁇ l 5% w/v 4-hydroxybenzhydrazide (Sigma H9882, prepared in 0.5 N HCl) with 80 ⁇ l 0.5 N NaOH followed by 20 ⁇ l of amylase reaction in an full skirt PCR plate (Axygen PCR-96-FS-C). The plate was sealed (Microseal B adhesive sealer, BioRad MSB-1001) and incubated at 95C for 2 minutes followed by immediate cooling to 25C on a PCR style thermocycling heating block. 80 ⁇ l of reaction sample was transferred to a polystyrene 96 well microtiter plate and the optical density was measured at 440 nm using a Spectramax plate reader.
  • Total glucose present in amylase reactions was determined in a microtiter plate by mixing 20 ⁇ l of reaction sample with 50 ⁇ l 5.8 mg/ml 2,2'-Azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt (Sigma, A1888) in 50 mM potassium phosphate buffer pH 6.8, containing 0.005% v/v Tween 80 followed by addition of 30 ⁇ l solution containing 0.33 U/ml peroxidase from horse radish type VI (Sigma, P8375), 3.33 U/ml OxyGo (Glucose Oxidase, Genencor) prepared in the same buffer. The microtiter plate was immediately placed in a Spectramax plate reader, shaken for 5 seconds and the optical denisity was monitored at 405 nm at 9 second intervals for the time period of 60-180 seconds.
  • Iodine analysis of amylase reactions was performed by mixing a 1:4 dilution (in water) of amylase reaction sample with 80 ⁇ l of Lugols reagent (5 g iodine, 10 g potassium iodide dissolved in 100 ml water) diluted 1:20 in water in a polystyrene microtiter plate.
  • Lugols reagent 5 g iodine, 10 g potassium iodide dissolved in 100 ml water
  • Optical density at 580 nm was determined using a Spectramax plate reader.
  • Microsoft Excel was used to assemble data acquired from the Softmax Pro software (plate reader).
  • Iodine results are reported as total OD580; chain length/residual amylose is a function of total OD, therefore amylase activity is inversely proportional to total OD.
  • Total reducing sugars are reported as total OD440 and are proportional to OD therefore amylase activity is directly proportional to OD.
  • Total glucose is reported as a kinetic rate in the glucose assay and is directly proportional.
  • OD and rates are reported in lieu of converting to known quantities using standard curves constructed from glucose. Ratios are reported using raw data and are therefore unit-less. The three types of data were combined graphically, as a ratio of iodine divided by the ratio of total reducing sugars to glucose.
  • a high-throughput viscometry assay was developed using the commercially available molecular rotor CCVJ (9-(2-carboxy-2-cyanovinyl) julolidine).
  • a molecular rotor is a fluorescent species whose quantum yield (the number of photons emitted divided by the number of photons absorbed) is dependent on the free volume of the microenvironment, which is related in turn to viscosity.
  • intramolecular rotation is the preferred mode of relaxation from the excited state. Intramolecular rotation is inhibited in a manner proportionate to the viscosity of the microenvironment, the balance of energy being dissipated through radiative relaxation (fluorescent emission).
  • the molecular rotor CCVJ was incorporated into a buffered suspension of corn amylopectin as follows.
  • a 100 mM stock solution of CCVJ was prepared by adding 186 ⁇ l of dimethyl sulfoxide to a vial containing 5 mg of lyophilized CCVJ (Sigma Aldrich Corporation, St. Louis, MO).
  • the CCVJ stock solution was stored in the dark at room temperature and checked for precipitation prior to use.
  • 90 g of amylopectin from corn (MP Biomedicals LLC, Solon, OH) were added to 2,850 mL of distilled water.
  • Spectramax M2e fluorometer (Molecular Devices Corporation, Sunnyvale, CA) that was set up as follows: top-read fluorescence mode; excitation wavelength 435 nanometers (nm); emission wavelength 495 nm; cutoff wavelength 455 nm; kinetic read mode with 24-second read interval; 15-second shake before initial read, 3-second shake between reads; 192 seconds total read time with a 20-second lag period (eliminating from each kinetic rate calculation the first of the 9 data points collected).
  • the molecular rotor CCVJ was incorporated into a buffered slurry of corn flour as follows.
  • a 100 mM stock solution of CCVJ was prepared by adding 186 ⁇ l of dimethyl sulfoxide to a vial containing 5 mg of lyophilized CCVJ (Sigma Aldrich Corporation, St. Louis, MO).
  • the CCVJ stock solution was stored in the dark at room temperature and checked for precipitation prior to use.
  • Organic corn flour (Azure Farm, Dufur, OR) was passed through a 600-micrometer sieve, then baked at 95 degrees C for 16 hours and returned to room temperature.
  • a 20% (weight/weight), pH 5.8 corn flour slurry was prepared in 2-kg batches by combining 1520 g of distilled water, 80 mL of 1 M sodium acetate buffer pH 5.6 (previously prepared by titrating 1 molar sodium acetate with 1 molar acetic acid), 80 ⁇ l of Tween-80 (Sigma Aldrich Corporation, St. Louis, MO), 80 ⁇ l of the 100 mM CCVJ stock solution, and 400 g of sifted organic corn flour. The slurry was stirred vigorously and continuously for half an hour using a magnetic stir bar, at which point the pH was checked and confirmed to be 5.8.
  • the slurry was stirred vigorously and continuously to keep the corn flour uniformly dispersed, while 90 ⁇ l of slurry were added to each well of a black untreated polystyrene 96-well microtiter plate (Corning Incorporated, Corning, NY) using a multichannel pipet with 200- ⁇ l tips trimmed to an inner diameter of approximately 2.3 millimeters, determined by vernier caliper (Mitutoyo Corporation, Kure, Hiroshima, Japan).
  • a decrease in fluorescent signal corresponded to a decrease in the density of the gelatinized corn flour, which in turn corresponded to an increase in liquefaction due to enzymatic activity.
  • the specific activity and pH optima of full-length AmyE (SEQ ID NO: 1), AmyE-tr (SEQ ID NO: 2), and variants, thereof, were measured using assays described in Example 2.1.
  • the specific activities were determined by spectrophotometrically determining the amount of dye released from a RBB-corn starch substrate over 30 minutes at 50°C and pH 4.5, 5.0, and 5.6.
  • FIG. 3 shows that AmyE-tr and Amy31A have highest specific activities at pH 4.5, compared to pH 5 or 5.6.
  • AmyE shows a higher specific activity at pH 5 than at pH 5.6.
  • AmyE, AmyE-tr, and variants, thereof, to reduce the viscosity of a corn starch substrate was determined using the assay method described in Example 2.2. The viscosity was measured as a function of time at pH 4.5 and 5.8 for each enzyme.
  • FIG. 4A and 4B respectively, show that AmyE-tr and AmyE reduced substrate viscosity at both pH 4.5 and 5.8. The peak viscosities were the same, while a lower final viscosity was observed at pH 5.8.
  • FIG. 4C and 4D respectively, show that Amy31A has a better performance at pH 4.5 than pH 5.8.
  • FIG. 5A shows the DSC unfolding profiles for AmyE and AmyE-tr, with and without 2 mM Ca 2+ .
  • FIG. 5B shows the DSC unfolding profiles for full length Amy31A variant.
  • the absence of any effect of calcium on the thermal melting points suggests that neither AmyE, AmyE-tr, nor Amy31 A bind Ca 2+ or are stabilized by Ca 2+ in the mM concentration range. Contrasting results were obtained for G.
  • AmyS stearothermophilus ⁇ -amylase
  • AmyE-tr SEQ ID NO: 2
  • six AmyE variants of position Q153 (C, F, I, K, N, and V) of AmyE-tr to convert maltose and maltoheptaose substrates to glucose at pH 5.6 was tested, using the glucose formation assay described in Example 2.3. Glucose generated was measured after 1, 2, and 3 days. AmyE-tr and AmyE variants were used at 1 ppm. Truncated AmyS (SEQ ID NO: 4) was used for comparison at a similar dose.
  • FIG. 6 depicts the results of glucose production from a maltose substrate.
  • the production of glucose by AmyS was minimal, while AmyE-tr and the Q153 position variants produced significant amounts of glucose.
  • the variant Q153N was the best producer of glucose under these conditions.
  • FIG. 7 depicts the results of glucose production from a maltoheptaose substrate.
  • AmyS converted maltoheptaose to glucose with poor efficiency.
  • AmyE-tr and Q153 position variants converted maltoheptaose to glucose very effectively, with Q153K and F variants displaying the greatest conversion by day 3.
  • This example demonstrates that AmyE and a variant of AmyE efficiently produce glucose from complex oligosaccharides.
  • FIG. 8 shows that AmyE-tr converts DP7 predominately to DP1 and residual amounts of maltose (DP2) after a 72h incubation.
  • FIG. 9 shows that AmyS converts DP7 to smaller oligosaccharides over time, producing a mixture of DP5, DP4, DP3, DP2 and DP1 oligosaccharides.
  • FIG. 10 depicts a time course of the conversion of DP7 to smaller oligosaccharides in the presence of AmyE variant Q153K. Significant levels of DP1, DP2, and DP3 were detected in as little as 1 h. By 3 h, the Q153K variant converted DP7 predominately to DP1.
  • This example relates to the generation and expression of a library of positional variants.
  • Plasmid pME630.7 ( FIG. 2 , Example 1) was used to generate positional libraries at 150 different amino acid residues of AmyE-tr. Table 2 lists each residue for which a positional library was made. Residues are numbered based on their position in SEQ ID NO: 2. The amino acid listed at each position is the residue appearing in the AmyE of SEQ ID NO: 2 (i.e., the wild type residue). Table 2 Variants No. SEQ ID NO:2 Numbering Wild type residue Variant No. SEQ ID NO:2 Numbering Wild type residue Variant No.
  • the positional library for each of the 150 residues listed on Table 1 contained approximately 16 amino acid substitution variants.
  • the libraries consisted of transformed B . subtilis cells containing expression plasmids encoding AmyE variant sequences at the 150 positions described. Each variant was confirmed by DNA sequencing analysis prior to protein activity evaluation. Individual clones were cultured as described below to obtain the different AmyE variants for functional characterization.
  • the B. subtilis transformants containing AmyE substitution variants were cultured in 96 well plates for 8 hours in LB (Luria broth) with 10 ⁇ g/ml neomycin, and 30 ⁇ l of this pre-culture was added to a 250 mL flask filled with 30 mL of cultivation media (described below) supplemented with 25 ppm chloramphenicol and 5 mM CaCl 2 .
  • the flasks were incubated for 60-65 hours at 37°C with constant rotational mixing at 250 rpm. Cultures were harvested by centrifugation at 5,000 rpm. for 20 minutes in conical tubes. The culture supernatants were used for assays.
  • the cultivation media was an enriched semi-defined media based on MOPs buffer, with urea as major nitrogen source, glucose as the main carbon source, and supplemented with 1% soytone for robust cell growth.
  • the AmyE position variants were evaluated using a starch hydrolysis assay to measure specific activity and thermal stability. AmyE variants also were assayed using a cleaning swatch assay to measure stain removal performance.
  • the pH stability of AmyE variants was evaluated by measuring amylase activity on a maltoheptaose substrate. Thermostability of each of the AmyE variants was determined by measuring amylase activity on a maltotriose substrate before and after heat stress.
  • a starch hydrolysis assay was used to measure specific activity and stability of AmyE and AmyE variants. Conditions that closely mimic real-world applications in cleaning and grain processing were used. Activity is defined as reducing ends generated by enzymatic breakdown of corn flour. Reducing ends were determined using a PAHBAH (p-hydroxybenzoic acid hydrazide) assay, described below. Stability is defined as sustained activity at 80°C.
  • PAHBAH p-hydroxybenzoic acid hydrazide
  • PAHBAH assay Aliquots of 80 ⁇ L of 0.5 N NaOH were added to all wells of an empty PCR plate (a "PAHBAH reaction plate"), followed by 20 ⁇ L of PAHBAH reagent (5% w/v p-hydroxybenzoic acid hydrazide (Sigma # H9882, St. Luois, MO, USA), dissolved in 0.5 N HCl). The solutions were mixed by pipetting up and down. 10 ⁇ L of the starch hydrolysis reaction supernatants were added to each well of the PAHBAH reaction plate. The plates were sealed and placed in a thermocycler, programmed for 2 minutes at 95°C, and then cooled to 20°C. Samples of 80 ⁇ L of the developed PAHBAH reaction mixtures were transferred to a fresh plate, and absorbance was measured at 405 nm in a spectrophotometer.
  • the stain removal performance of AmyE and AmyE variants was determined using CS-28 rice starch stain microswatches. Microswatches of 1 ⁇ 4-inch circular diameter were obtained from CFT Vlaardingen (Netherlands). Two microswatches were placed into each well of a 96-well microtiter plate.
  • the filtered culture broth samples were tested at an appropriate concentration by dilution with a mixture of 10 mM NaCl, 0.1 mM CaCl 2 , 0.005% Tween-80 to 20x the desired final concentration in the performance test.
  • the final concentration of enzyme was about 0.025-0.10 ppm.
  • Amylase performance was measured at both pH 8 and pH 10.
  • Either 190 ⁇ l of (A) a buffer solution containing 25 mM HEPES (Sigma, H7523), 2 mM CaCl 2 , 0.005% Tween-80, pH 8.0, or (B) a buffer solution containing 25 mM CAPS (Sigma, C2632), 2 mM CaCl 2 , 0.005% Tween-80, pH 10.0 were added to each well of the plates containing microswatches. 10 ⁇ l of diluted amylase samples were added to each well to provide a total volume of 200 ⁇ l/well. The plate was covered with a plate seal and placed in an iEMS incubator for 60 minutes at 40°C with agitation at 1,150 rpm.
  • Variants with performance differences over the wild-type enzyme were characterized by a performance index (PI).
  • PI performance index
  • a PI less than 1 (PI ⁇ 1) identified a variant that performs worse than the standard.
  • amylase activity assay using maltoheptaose as a substrate was used to determine pH stability of AmyE and AmyE variants.
  • Alpha amylase activity was measured by monitoring production of glucose at pH 5.8 and pH, 4, using an enzyme-coupled colorimetric kinetic assay. Enzyme reactions were carried out in flat-bottom polystyrene 96-well microtiter plates at room temperature.
  • Reactions were initiated by the addition of 50 ⁇ l of buffer containing 50 mM sodium acetate, pH 5.8, 5.4 mg/ml 2,2'-Azino-bis (3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt (Sigma-Aldrich, cat. # A1888) and 10 mM maltoheptaose (Sigma-Aldrich, cat. # M7753), and was followed by 5 seconds of mixing. Color formation in the reaction was monitored at 405 nm in 9 second intervals for 240 seconds using a SpectraMAX 250 spectrophotometer (Molecular Devices, Union City, CA). Enzyme activity was reported as the rate of color formation during the 120-240 second interval of monitoring.
  • thermostability of AmyE and AmyE variants was measured by determining the amylase activity on maltotriose substrate at pH 5.8, monitoring the production of glucose using an enzyme-coupled colorimetric kinetic assay.
  • the assay method used here was the same as described above using the maltoheptaose substrate.
  • a 20 ⁇ l sample of diluted culture supernatants of AmyE or AmyE variants were used, and color formation was monitored during the 60-180 second interval of the reactions.
  • 80 ⁇ l samples of diluted cultures were then transferred to fresh plates, fitted with plate sealers, and incubated for 30 minutes at 60 °C with 650 rpm shaking on an iEMS device (Thermo Fisher Scientific, Inc., Waltham, MA).
  • the performance index was calculated by dividing the activity of the variant by the activity of the wild-type enzyme. The performance index compared the performance of the variant (actual value) and the standard AmyE reference enzyme (theoretical value) at the same protein concentration.
  • Flasks were incubated at 32°C with stir bars at 320 rpm for 48h fermentation. The amount of ethanol produced was measured by HPLC analysis. The performance of truncated AmyE (SEQ ID NO: 2) was compared to SPEZYME® Xtra amylase (SEQ ID NO: 4) at pH 4.3 and pH 5.8. Truncated AmyE and SPEZYME® Xtra amylase were dosed at 0.2 mg/gDS.
  • the final ethanol yield produced by truncated AmyE at pH 5.8 is 12.0% (v/v).
  • Truncated AmyE at pH 4.3 yielded a final ethanol yield of 7.3% (v/v).
  • Final ethanol yields in the presence of SPEZYME® Xtra amylase were 2.7% (v/v) at pH 4.3 and 3.9% (v/v) at pH 5.8.
  • a . kawachii alpha amylase (AkAA, GC626), dosed at 1.5 SSU/g (one unit of the enzyme activity-SSU soluble starch unit is equivalent to the reducing power of 1 mg of glucose released per minute from the hydrolyssi of soluble potato starch substrate (4%ds) at pH 4.5 and 50°C) and STARGENTM 002 ( Aspergillus kawachi alpha amylase expressed in Trichoderma reesei and a glucoamylase from Trichoderma reesei that work synergistically to hydrolyze granular starch substrate to glucose), dosed at 0.5 GAU/g, where one Glucoamylase Unit (GAU) is the amount of enzyme that will produce 1 ⁇ M of reducing sugar, calculated as glucose per hour from a soluble starch substrate (4% ds) at pH 4.2 and 60°
  • GAU Glucoamylase Unit
  • FIG. 12 shows the results observed when performance of these enzymes were compared, at pH 4.3 and 5.8, and reported as final ethanol yield produced.
  • both full length and truncated AmyE performed very comparably to the STARGEN TM 002, with full length AmyE actually surpassing the ethanol yields observed for Stargen TM 002 at pH 4.3.
  • the truncated AmyE when tested at pH 5.8 performed very comparably to Stargen TM 002 tested at the same pH.
  • the A . kawachii alpha amylase performed very poorly at both pH 4.2 and pH 5.8.
  • B. subtilis AmyE full length SEQ ID NO: 1
  • AmyE truncated SEQ ID NO: 2
  • variant ⁇ -amylase Amy 31A SEQ ID NO: 3
  • AmyS truncated Geobacillus stearothermophilus ⁇ -amylase
  • Purified Amy E (24.5 g/L) was diluted to a final concentration of 20.4 ppm in malic acid buffer, pH 5.6. The protein was then added to a 5% corn flour solution in malic acid buffer, pH 5.6 to a final concentration of 1 ppm. The mixture was then incubated in a shaker at 32°C. Samples were periodically removed and diluted into 50mM NaOH to quench the reaction. 10 ⁇ L samples were then injected into an HPLC system (Agilent 1000) enabled with electrochemical detection. A PA1 column was used with a gradient of NaOH and Na-acetate run at 25°C. The distribution was determined from previously run standards.
  • Viscosity reduction of corn flour due to the action of the ⁇ -amylase was monitored using a HAAKE Viscotester 550 instrument.
  • the substrate slurry is made up fresh daily in batch mode with 30% corn flour dry solids.
  • the pH was adjusted to 5.8 using sulfuric acid.
  • 50 g of the slurry (15 g dry solids) is weighed out and pre-incubated, with stirring, for 10 minutes to warm up to 70°C.
  • the temperature is immediately ramped up from 70°C to 85°C with a rotation speed of 75 rpm. Once the temperature of the slurry and enzyme mixture reaches 85°C, its temperature is held constant and viscosity is monitored for an additional 30 minutes. The viscosity was measured throughout the run and is reported in ⁇ Nm.
  • Wild-type AmyE full-length or truncated
  • several variants, thereof were dosed at from about 0.25 to 1.5 mg/50 g of corn flour slurry and the viscosity recorded.
  • FIG 15 A typical graph of the viscosity of the slurry over time is shown in FIG 15 , in which the wild-type full-length AmyE, and the AmyE full-length variants I100F and W60M are compared. In other cases, only the peak and final viscosity of the slurry are tabulated.
  • the results for wild-type, full-length AmyE, and the variants L142F, L142G, L142Q, L142S, L142W, L142Y, A214I, A214V, S245Y, Q126F, Q126L, Q126P, Q126V, S131L, and S254I, made in the full-length AmyE background, are shown in Tables 3 and 4.
  • Peak and final viscosity obtained using truncated wild-type and variant AmyE (corn flour bag F) dose (mg) peak viscosity final viscosity WT 1.40 27300 1490 L142F 0.60 26100 550 L142G 0.30 29900 1925 L142Q 0.30 31400 2800 L142S 0.25 30000 2495 L142W 1.40 33000 570 L142Y 1.20 27800 1940 A214I 1.40 24700 2330 A214V 1.40 21700 560 S245Y 1.40 25800 520 Q126F 0.70 32300 2540 Q126L 1.40 30900 400 Q126P 1.40 25100 480 Q126V 1.40 28300 520 S131L 1.40 26100 450 Table 4.
  • Peak and final viscosity obtained using truncated wild-type and variant AmyE (corn flour bag G) dose (mg) peak viscosity final viscosity WT 0.60 33600 890 L142F 0.45 28000 700 L142G 0.30 25300 2620 L142Q 0.30 26300 4320 L142S 0.25 31200 11200 L142Y 0.60 28600 570 A214I 0.60 25200 780 Q126F 0.50 32400 2020 S254I 0.60 32500 1320 Table 5.
  • Peak and final viscosity obtained using truncated wild-type and variant AmyE (corn flour bag H) dose (mg) peak viscosity final viscosity WT 1.40 29800 840 W60L 0.75 29200 1980 W60M 1.00 29100 2220 W60N 1.00 30900 4250 I100F 0.75 29600 870 I100M 0.75 29200 840 S105M 0.75 30300 2170 S105W 0.75 30400 1960 G207A 0.75 29300 1920 T270A 0.75 31100 1540 T270E 1.00 33200 1300 T270L 0.85 33000 1520 T270N 1.40 27700 560 T270V 0.80 33900 2400 T279A 0.75 29400 1280
  • Improved performance in the viscometer assay can be identified using a number of criteria, i.e., decreased peak viscosity, decreased final viscosity, or a decreased enzyme dose required to produce similar peak or final viscosities relative to the dose required for a reference (control) enzyme.
  • criteria i.e., decreased peak viscosity, decreased final viscosity, or a decreased enzyme dose required to produce similar peak or final viscosities relative to the dose required for a reference (control) enzyme.
  • the bold highlighted text in Tables 4-5 indicate the criteria in which each variant demonstrates improved performance compared to the respective wild-type control.
  • T m The thermal midpoint (T m ) of the DSC curves was used as an indicator of the thermal stability.
  • Table 6 shows the T m values of wildtype truncated AmyE and truncated AmyE variants tested at pH 4.0 and pH 5.8.

Claims (4)

  1. Procédé destiné à la production d'éthanol à partir d'un substrat d'amidon, comprenant :
    la liquéfaction et la saccharification d'un substrat d'amidon afin de produire du glucose en faisant rentrer en contact ledit substrat d'amidon avec un polypeptide AmyE ayant la séquence de SEQ ID No: 1, SEQ ID No: 2 ou SEQ ID No: 3.
    dans lequel la liquéfaction et la saccharification sont réalisées dans le même mélange réactionnel sans ajustement du pH,
    ledit procédé comprenant en outre la fermentation dudit glucose pour produire de l'éthanol.
  2. Procédé selon la revendication 1, dans lequel au moins une partie de la saccharification et de la fermentation a lieu dans le même mélange réactionnel simultanément.
  3. Procédé selon la revendication 1, dans lequel du calcium exogène n'est pas ajouté au mélange réactionnel.
  4. Procédé selon la revendication 1, dans lequel la concentration de calcium dans le mélange réactionnel est inférieure à environ 8 ppm.
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EP2297312B1 (fr) 2013-09-04
JP2014168469A (ja) 2014-09-18
JP2011522546A (ja) 2011-08-04
WO2009149395A3 (fr) 2010-03-25
MX2010013114A (es) 2011-04-05
ES2538406T3 (es) 2015-06-19
CN102131924A (zh) 2011-07-20
MX350760B (es) 2017-09-18
DK2297312T3 (da) 2013-12-16
WO2009149419A2 (fr) 2009-12-10
CN103773749A (zh) 2014-05-07
CA2726803A1 (fr) 2009-12-10
HUE025251T2 (en) 2016-02-29
US20100003366A1 (en) 2010-01-07
CA2726274C (fr) 2018-11-20
BRPI0915606A2 (pt) 2021-03-09
US20100015686A1 (en) 2010-01-21
JP5933619B2 (ja) 2016-06-15
PL2297313T3 (pl) 2015-08-31
WO2009149395A2 (fr) 2009-12-10
US8323945B2 (en) 2012-12-04
CN102112605A (zh) 2011-06-29
EP2297313A2 (fr) 2011-03-23
US20160010129A1 (en) 2016-01-14
MX2010013123A (es) 2011-01-14
US20130149770A1 (en) 2013-06-13
WO2009149419A3 (fr) 2010-04-22
CN102131924B (zh) 2017-06-09
US9090887B2 (en) 2015-07-28
BRPI0913367A2 (pt) 2015-08-04
DK2297313T3 (en) 2015-06-08
US8975056B2 (en) 2015-03-10
JP2011525350A (ja) 2011-09-22
MX364987B (es) 2019-05-17
CN102112605B (zh) 2014-02-26
EP2297312A2 (fr) 2011-03-23
CA2726274A1 (fr) 2009-12-10

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